A novel nonsense mutation in the MIP gene linked to congenital posterior polar cataracts in a Chinese family

Abstract

Purpose: To detect the causative mutation for congenital posterior polar cataracts in a five-generation Chinese family and further explore the potential pathogenesis of this disease. Methods: Coding exons, with flanking sequences of five candidate genes, were screened using direct DNA sequencing. The identified mutations were confirmed by restriction fragment length polymorphism (RFLP) analysis. A full-length wild-type or an Y219∗ mutant aquaporin0 (AQP0) fused with an N-terminal FLAG tag, was transfected into HEK293T cells. For colocalization studies, FLAG-WT-AQP0 and Myc-Y219∗-AQP0 constructs were co-transfected. Quantitative real-time RT-PCR, western blotting and immunofluorescence studies were performed to determine protein expression levels and sub-cellular localization, respectively. Results: We identified a novel nonsense mutation in MIP (c.657 C>G; p.Y219∗) (major intrinsic protein gene) that segregates with congenital posterior polar cataract in a Chinese family. This mutation altered a highly conserved tyrosine to a stop codon (Y219∗) within AQP0.When FLAG-WT-AQP0 and FLAG-Y219∗-AQP0 expression constructs were singly transfected into HEK 293T cells, mRNA expression showed no significant difference between the wildtype and the mutant, while Y219∗-AQP0 protein expression was significantly lower than that of wild-type AQP0. Wild-type AQP0 predominantly localized to the plasma membrane, while the mutated protein was abundant within the cytoplasm of HEK293T cells. However, when FLAG-WT-AQP0 and Myc-MU-AQP0were co-expressed, both proteins showed high fluorescence in the cytoplasm. Conclusions: The novel nonsense mutation in the MIP gene (c.657 C>G) identified in a Chinese family may cause posterior polar cataracts. The dominant negative effect of the mutated protein on the wild-type protein interfered with the trafficking of wild-type protein to the cell membrane and both the mutant and wild-type protein were trapped in the cytoplasm. Consequently, both wild-type and mutant protein lost their function as a water channel on the cell membrane, and may result in a cataract phenotype. Our data also expands the spectrum of known MIP mutations.